510(k) K260140
- Device
- Aevice Wheeze Detection Module
- Applicant
- Aevice Health Pte. , Ltd.
- 510(k) number
- K260140
- Product code
- PHZ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2026-09-25
- Date received
- 2026-01-20
- Regulation
- 868.1900
- Classification name
- Abnormal Breath Sound Device
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- N
Applicant Contact#
- Contact
- Adrian Ang
- Address
- 3 Tai Seng Ave., Tai Seng Exchange Tower B #04-32 Singapore SG 536465 536465
FDA Registration Numbers#
- 3012678246
- 3021974922
Source Documents#
Other 510(k) Records For Product Code PHZ#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K252844 | Tyto Insights for Wheeze Detection (with PCCP) | Tyto Care , Ltd. | 2026-06-02 |
| K243567 | Tyto Insights for Rhonchi Detection | Tyto Care , Ltd. | 2025-04-07 |
| K240555 | Tyto Insights for Crackles Detection | Tyto Care , Ltd. | 2024-07-02 |
| K232237 | Tyto Insights for Wheeze Detection | Tyto Care , Ltd. | 2023-12-13 |
| K221614 | TytoCare Lung Sounds Analyzer | Tyto Care , Ltd. | 2023-02-24 |
| K202062 | wheezo WheezeRate Detector | Respiri Limited | 2021-03-11 |
| K131285 | SONOSENTRY | Isonea, Ltd. | 2014-08-19 |